Removing the threat of diclofenac to critically endangered Asian vultures

被引:128
作者
Swan, G
Naidoo, V
Cuthbert, R
Green, RE [1 ]
Pain, DJ
Swarup, D
Prakash, V
Taggart, M
Bekker, L
Das, D
Diekmann, J
Diekmann, M
Killian, E
Meharg, A
Patra, RC
Saini, M
Wolter, K
机构
[1] Univ Pretoria, Fac Vet Sci, Dept Paraclin Sci, ZA-0110 Onderstepoort, South Africa
[2] Univ Pretoria, Fac Vet Sci, Ctr Biomed Res, ZA-0110 Onderstepoort, South Africa
[3] Royal Soc Protect Birds, Sandy SG19 2DL, Beds, England
[4] Univ Cambridge, Dept Zool, Conservat Biol Grp, Cambridge CB2 1TN, England
[5] Indian Vet Res Inst, Izatnagar 243122, Uttar Pradesh, India
[6] Bombay Nat Hist Soc, Bombay, Maharashtra, India
[7] Univ Aberdeen, Sch Biol Sci, Dept Plant & Soil Sci, Aberdeen AB9 1FX, Scotland
[8] Rare & Endagered Species Trust, Otjiwarongo, Namibia
[9] DeWildt Cheetah & Wildlife Trust, Vulture Unit, Hartbeespoort, South Africa
关键词
D O I
10.1371/journal.pbio.0040066
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Veterinary use of the nonsteroidal anti-inflammatory (NSAID) drug diclofenac in South Asia has resulted in the collapse of populations of three vulture species of the genus Gyps to the most severe category of global extinction risk. Vultures are exposed to diclofenac when scavenging on livestock treated with the drug shortly before death. Diclofenac causes kidney damage, increased serum uric acid concentrations, visceral gout, and death. Concern about this issue led the Indian Government to announce its intention to ban the veterinary use of diclofenac by September 2005. Implementation of a ban is still in progress late in 2005, and to facilitate this we sought potential alternative NSAIDs by obtaining information from captive bird collections worldwide. We found that the NSAID meloxicam had been administered to 35 captive Gyps vultures with no apparent ill effects. We then undertook a phased programme of safety testing of meloxicam on the African white-backed vulture Gyps africanus, which we had previously established to be as susceptible to diclofenac poisoning as the endangered Asian Gyps vultures. We estimated the likely maximum level of exposure (MLE) of wild vultures and dosed birds by gavage (oral administration) with increasing quantities of the drug until the likely MLE was exceeded in a sample of 40 G. africanus. Subsequently, six G. africanus were fed tissues from cattle which had been treated with a higher than standard veterinary course of meloxicam prior to death. In the final phase, ten Asian vultures of two of the endangered species (Gyps bengalensis, Gyps indicus) were dosed with meloxicam by gavage; five of them at more than the likely MLE dosage. All meloxicam-treated birds survived all treatments, and none suffered any obvious clinical effects. Serum uric acid concentrations remained within the normal limits throughout, and were significantly lower than those from birds treated with diclofenac in other studies. We conclude that meloxicam is of low toxicity to Gyps vultures and that its use in place of diclofenac would reduce vulture mortality substantially in the Indian subcontinent. Meloxicam is already available for veterinary use in India.
引用
收藏
页码:395 / 402
页数:8
相关论文
共 38 条
[1]  
Anderson MD, 2005, S AFR J SCI, V101, P112
[2]   Comparative pharmacokinetics of three non-steroidal anti-inflammatory drugs in five bird species [J].
Baert, K ;
De Backer, R .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY C-TOXICOLOGY & PHARMACOLOGY, 2003, 134 (01) :25-33
[3]   Renal effects of cyclooxygyenase-2-selective inhibitors [J].
Brater, DC .
JOURNAL OF PAIN AND SYMPTOM MANAGEMENT, 2002, 23 (04) :S15-S20
[4]   Evaluation of intravenous administration of meloxicam for perioperative pain management following stifle joint surgery in dogs [J].
Budsberg, SC ;
Cross, AR ;
Quandt, JE ;
Pablo, LS ;
Runk, AR .
AMERICAN JOURNAL OF VETERINARY RESEARCH, 2002, 63 (11) :1557-1563
[5]  
CAMIFIA A, 2001, 4 EUR C RAPT SEV SPA, P34
[6]  
Clyde Victoria L., 1999, P309
[7]  
CUNNINGHAM AA, 2001, 4 EUR C RAPT 2001 25, P10
[8]   Efficacy and tolerability of meloxicam, a COX-2 preferential nonsteroidal anti-inflammatory drug - A review [J].
Del Tacca, M ;
Colucci, R ;
Fornai, M ;
Blandizzi, C .
CLINICAL DRUG INVESTIGATION, 2002, 22 (12) :799-818
[9]   Analgesic comparison of meloxicam or ketoprofen for orthopedic surgery in dogs [J].
Deneuche, AJ ;
Dufayet, C ;
Goby, L ;
Fayolle, P ;
Desbois, C .
VETERINARY SURGERY, 2004, 33 (06) :650-660
[10]  
DEVOS V, 1994, INFECT DIS LIVESTOCK, P1262